NM_022167.4(XYLT2):c.166G>A (p.Asp56Asn) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002073413.5
Allele description [Variation Report for NM_022167.4(XYLT2):c.166G>A (p.Asp56Asn)]
NM_022167.4(XYLT2):c.166G>A (p.Asp56Asn)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 26, 2024